Abstract
Background
Analysis of the National Cancer Institute’s Surveillance, Epidemiology, and End Results data has shown that the incidence of thyroid cancer is higher in patients with a preexisting malignancy and that the incidence of other malignancies is higher in patients with thyroid cancer. The purpose of this study was to evaluate the prevalence of a second malignancy in patients treated for thyroid, breast or renal cell cancer and determine what associations, if any, exist between these cancers.
Methods
This study utilized the novel data system, Explorys, as its population base. Patient cohorts were constructed using ICD-9 codes, and prevalence rates were obtained for each cancer. Rates of second malignancy were obtained and compared to the baseline prevalence for a particular malignancy.
Results
Female thyroid cancer patients had a 0.67- and twofold increase in prevalence of a subsequent breast and renal cell cancer. Female breast and renal cell cancer patients had a twofold and 1.5-fold increase in the prevalence of thyroid cancer, respectively. Male patients with thyroid cancer had a 29- and 4.5-fold increase in prevalence of subsequent breast and renal cell cancer. Male patients with breast and renal cell cancer had an increased prevalence of subsequent thyroid cancer, 19- and threefold, respectively.
Conclusions
Our study demonstrated a bidirectional association between thyroid, breast and renal cancer in both male and female patients. This may have important implications for patient follow-up and screening after treatment of a primary cancer.
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Acknowledgment
We would like to thank the Explorys team for their expertise: Anil Jain, MD, Jason Gilder, PhD, Wendy Foster, MPH, RHIA and Sarah Mihalik, Heather Holmes, Clinical Informationalist, Summa Health System, and Steve Getch, Corporate Communications, Summa Health System.
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Van Fossen, V.L., Wilhelm, S.M., Eaton, J.L. et al. Association of Thyroid, Breast and Renal Cell Cancer: A Population-based Study of the Prevalence of Second Malignancies. Ann Surg Oncol 20, 1341–1347 (2013). https://doi.org/10.1245/s10434-012-2718-3
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DOI: https://doi.org/10.1245/s10434-012-2718-3